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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 221478생성일: 2026년 10월 26일

Methyl chloroacetate → 7-tert-Butyl 1-methyl 3-(trifluoromethyl)-5H,6H,7H,8H-imidazo[1,5-a]pyrazine-1,7-dicarboxylate

https://huagongshe.com/reaction/221478

반응식

참여 물질

역할이름HCID투입량
반응물Methyl chloroacetateHCID 7295—
반응물Potassium CarbonateHCID 11430—
반응물tert-butyl 1-bromo-3-(trifluoromethyl)-5H,6H,7H,8H-imidazo(1,5-a)pyrazine-7-carboxylateHCID 57518451—
촉매Dicobalt Octacarbonyl (stabilized with 1-5% Hexane)HCID 25049—
용매MethanolHCID 887—
생성물7-tert-Butyl 1-methyl 3-(trifluoromethyl)-5H,6H,7H,8H-imidazo[1,5-a]pyrazine-1,7-dicarboxylateHCID 5751845267.8%

반응 단계

Octacarbonyldicobalt (5.54 g, 16.2 mmol) and potassium carbonate (11.2 g, 81.1 mmol) was dissolved in 100 mL of methanol under stirring. The reaction mixture was stirred for 15 minutes at 60° C., and 1-bromo-3-trifluoromethyl-5,6-dihydro-8H-imidazo[1,5-a]pyrazine-7-carboxylic acid tert-butyl ester 27b (3 g, 8.11 mmol) and methyl chloroacetate (5.25 g, 48.6 mmol) were then added to the solution. The reaction mixture was reacted for 6 hours under a carbon monoxide atmosphere and monitored by thin layer chromatography until the disappearance of the starting materials. After cooling to room temperature, the reaction mixture was filtered through a pad of silica gel, rinsed with methanol. The filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain the title compound 3-trifluoromethyl-5,6-dihydro-8H-imidazo[1,5-a]pyrazine-1,7-dicarboxylic acid 7-tert-butyl ester 1-methyl ester 27c (1.92 g, yield 67%) as a white solid. (Reference: J. Organomet. Chem, 1985, 293)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08207161B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-d14ccd8083c348e4b44b3ecc9a3d721c
출처 메모uspto-grants-2012_06